Parkinson disease. Parkinson disease
Conditions
Interventions
Intervention 1: Control group: Placebo, daily, for 12 weeks orally. Intervention 2: Intervention group: Omega-3 fatty acid plus vitamin E capsule, 1000 mg omega-3 fatty acid plus 400 IU vitamin E, dai
Sponsors
Kashan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
50 Years to 80 Years
Inclusion criteria
Inclusion criteria: Patients with Parkinson's; aged 50 to 80 years.
Exclusion criteria
Exclusion criteria: Subjects who were already taking omega-3 and/or vitamin E Subjects who were taking DDP4 inhibitors, statins and anti-inflammatory drugs Subjects who had depression and had severe psychosis.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Tumor necrosis factor alpha. Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: PCR.;Interleukin-1. Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: PCR.;Interleukin-8. Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: PCR. | — |
Secondary
| Measure | Time frame |
|---|---|
| Peroxisome proliferator–activated receptor ? (PPAR?). Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: PCR.;Low Density Lipoprotein Receptor (LDLR). Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: PCR. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactZatollah Asemi
Kashan University of Medical Sciences
Outcome results
None listed